OMIM.org: leveraging knowledge across phenotype–gene relationships

For over 50 years Mendelian Inheritance in Man has chronicled the collective knowledge of the field of medical genetics. It initially cataloged the known X-linked, autosomal recessive and autosomal dominant inherited disorders, but grew to be the primary repository of curated information on both gen...

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Detalles Bibliográficos
Autores principales: Amberger, Joanna S, Bocchini, Carol A, Scott, Alan F, Hamosh, Ada
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2019
Materias:
Database Issue
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6323937/
https://www.ncbi.nlm.nih.gov/pubmed/30445645
http://dx.doi.org/10.1093/nar/gky1151

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6323937/
https://www.ncbi.nlm.nih.gov/pubmed/30445645
http://dx.doi.org/10.1093/nar/gky1151

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